@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP489315.RABQ4yD5OHJrgn2_NW5E4AqvsctsoUnfjWI6TT-g6pVuE> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP489315.RABQ4yD5OHJrgn2_NW5E4AqvsctsoUnfjWI6TT-g6pVuE130_head {
  this: np:hasAssertion dgn-np:NP489315.RABQ4yD5OHJrgn2_NW5E4AqvsctsoUnfjWI6TT-g6pVuE130_assertion;
    np:hasProvenance dgn-np:NP489315.RABQ4yD5OHJrgn2_NW5E4AqvsctsoUnfjWI6TT-g6pVuE130_provenance;
    np:hasPublicationInfo dgn-np:NP489315.RABQ4yD5OHJrgn2_NW5E4AqvsctsoUnfjWI6TT-g6pVuE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP489315.RABQ4yD5OHJrgn2_NW5E4AqvsctsoUnfjWI6TT-g6pVuE130_assertion a np:Assertion .
  
  dgn-np:NP489315.RABQ4yD5OHJrgn2_NW5E4AqvsctsoUnfjWI6TT-g6pVuE130_provenance a np:Provenance .
  
  dgn-np:NP489315.RABQ4yD5OHJrgn2_NW5E4AqvsctsoUnfjWI6TT-g6pVuE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP489315.RABQ4yD5OHJrgn2_NW5E4AqvsctsoUnfjWI6TT-g6pVuE130_assertion {
  miriam-gene:7490 a ncit:C16612 .
  
  lld:C0007099 a ncit:C7057 .
  
  dgn-gda:DGNc5668698b1d6f19db6d872e31907a0f6 sio:SIO_000628 miriam-gene:7490, lld:C0007099;
    a sio:SIO_001121 .
}

dgn-np:NP489315.RABQ4yD5OHJrgn2_NW5E4AqvsctsoUnfjWI6TT-g6pVuE130_provenance {
  dgn-np:NP489315.RABQ4yD5OHJrgn2_NW5E4AqvsctsoUnfjWI6TT-g6pVuE130_assertion dcterms:description
      "[Low-grade dysplasia (18) and carcinoma in situ (12) associated with muscle-invasive urothelial carcinoma were microdissected and topographically analyzed (intraepithelial and invasive superficial and deep to muscularis mucosa) for methylation pattern of androgen receptor alleles, TP53, RB1, WT1, and NF1 microsatellite analysis to assess clonal identity; MLH1 and MSH2 sequencing/immunostaining.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:19368958;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP489315.RABQ4yD5OHJrgn2_NW5E4AqvsctsoUnfjWI6TT-g6pVuE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:52+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}